METHODS AND COMPOSITIONS FOR THE DETECTION AND ANALYSIS OF NUCLEIC ACIDS BY SIGNAL AMPLIFICATION
    2.
    发明申请
    METHODS AND COMPOSITIONS FOR THE DETECTION AND ANALYSIS OF NUCLEIC ACIDS BY SIGNAL AMPLIFICATION 审中-公开
    通过信号放大检测和分析核酸的方法和组合物

    公开(公告)号:WO2006092063A1

    公开(公告)日:2006-09-08

    申请号:PCT/CA2006/000322

    申请日:2006-03-03

    Abstract: The present invention relates to a novel integrated PCR-free signal amplification polynucleotide detection system which combines a specific receptor, an optical transducer, and an amplification mechanism. This novel detection system is based on different electrostatic interactions and conformations between a cationic polythiophene (i.e. polymer 1) and single-stranded or double-stranded polynucleotides (such as ss-DNA or ds-DNA), and the efficient energy transfer between the triplex (complexation between the cationic polythiophene and ds-DNA) and neighboring fluorophores attached to ss-DNA or ds-DNA probes. It is to be understood that in the case of ss-DNA, triplex formation occurs via the hybridization of complementary ss-DNA strands, combined with complexation with the cationic polythiophene. The present detection system allows for the detection of single nucleotide polymorphisms (SNPs) from samples in only a few minutes, without the need for nucleic acid amplification.

    Abstract translation: 本发明涉及一种结合特异性受体,光学换能器和放大机制的新型无PCR信号整合多聚核苷酸检测系统。 这种新型检测系统是基于阳离子聚噻吩(即聚合物1)和单链或双链多核苷酸(如ss-DNA或ds-DNA)之间的不同静电相互作用和构象,以及三链体之间的有效能量转移 (阳离子聚噻吩和ds-DNA之间的络合)和与ss-DNA或ds-DNA探针相连的相邻荧光团。 应当理解,在ss-DNA的情况下,通过互补的ss-DNA链的杂交与阳离子聚噻吩的络合结合发生三链体形成。 本检测系统允许仅在几分钟内从样品中检测单核苷酸多态性(SNPs),而不需要核酸扩增。

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